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Merck
所有图片(1)

文件

662141

Sigma-Aldrich

PR-619

≥99% (HPLC), solid, DUB inhibitor, Calbiochem®

别名:

DUB抑制剂V,PR-619, UCH-L3抑制剂II,UCH-L5/UCH37抑制剂III,USP5抑制剂II,USP7抑制剂I,USP9X抑制剂II,USP14抑制剂IV,USP14抑制剂IV,USP47抑制剂I,2,6-二氨基吡啶-3,5-双(硫氰酸盐),3,5-二硫氰基吡啶-2,6-二胺,PR619,UC

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About This Item

经验公式(希尔记法):
C7H5N5S2
分子量:
223.28
分類程式碼代碼:
12352200
NACRES:
NA.77

product name

DUB抑制剂V,PR-619, The DUB Inhibitor V, PR-619 controls the biological activity of DUB. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

品質等級

化驗

≥99% (HPLC)

形狀

solid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

light beige to yellow

溶解度

DMSO: 50 mg/mL

運輸包裝

ambient

儲存溫度

2-8°C

一般說明

一种细胞渗透性吡啶胺类广谱DUB抑制剂,其已知靶标包括ATXN3、BAP1、JOSD2、OTUD5、UCH-L1、UCH-L3、UCH-L5/UCH37、USP1、2、4、5、7、8、9X、10、14、15、16、19、20、22、24、28、47、48、VCIP135、YOD1,以及deISGylase PLpro、deNEDDylase DEN1和deSUMOlyase SENP6。PR-619和P22077(目录号662142)均显示以剂量和时间依赖性方式(20至150 µM;0.5至20 h)增加HEK293T细胞中的整体蛋白多聚泛素化,然而P22077暴露主要导致K48连接的富集,而PR619处理导致K48和K63连接的多聚亚基链的上调。

包裝

用惰性气体包装

警告

毒性:标准处理(A)

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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Alessandro Dario Confettura et al.
Translational neurodegeneration, 11(1), 2-2 (2022-01-07)
The metabolic syndrome is a consequence of modern lifestyle that causes synaptic insulin resistance and cognitive deficits and that in interaction with a high amyloid load is an important risk factor for Alzheimer's disease. It has been proposed that neuroinflammation
Kim Ghilarducci et al.
International journal of molecular sciences, 23(14) (2022-07-28)
Rab7 is a GTPase that controls late endosome and lysosome trafficking. Recent studies have demonstrated that Rab7 is ubiquitinated, a post-translational modification mediated by an enzymatic cascade. To date, only one ubiquitin E3 ligase and one deubiquitinase have been identified
Michelle Mølgaard Thomsen et al.
Journal of clinical immunology, 44(2), 56-56 (2024-01-26)
Varicella zoster virus (VZV) is a neurotropic alphaherpesvirus exclusively infecting humans, causing two distinct pathologies: varicella (chickenpox) upon primary infection and herpes zoster (shingles) following reactivation. In susceptible individuals, VZV can give rise to more severe clinical manifestations, including disseminated
Yaara Makaros et al.
Molecular cell, 83(11), 1921-1935 (2023-05-19)
Although most eukaryotic proteins are targeted for proteasomal degradation by ubiquitination, a subset have been demonstrated to undergo ubiquitin-independent proteasomal degradation (UbInPD). However, little is known about the molecular mechanisms driving UbInPD and the degrons involved. Utilizing the GPS-peptidome approach
Kim Ghilarducci et al.
The FEBS journal, 288(16), 4849-4868 (2021-03-03)
Protein ubiquitination has been historically associated with protein degradation, but recent studies have demonstrated other cellular functions associated with substrate ubiquitination. Among the RING-type ubiquitin E3 ligase enzymes present in the human genome, RNF167 is a transmembrane protein located in

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